A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575951



Internal ID16363360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:71240857..71282141hg38UCSC Ensembl
Innerchr17:69236998..69278282hg19UCSC Ensembl
Innerchr17:66748593..66789877hg18UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3841285
hg1941285
hg1841285
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv875927
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575951
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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